Adc®

FDA UDI

Class I (US FDA UDI)

by American Diagnostic Corporation

Identity

Trade Name: ADC® FDA UDI
Generic Name: Oropharyngeal airway, reusable FDA UDI
Device Name: Berman Airway, Medium, 80mm,Size 3, 12/pkg, Green FDA UDI
Model / Reference: 4080-12 FDA UDI
Description: Berman Airway, Medium, 80mm,Size 3, 12/pkg, Green FDA UDI

Identifiers

Catalog Number: 4080-12 FDA UDI
Primary DI / UDI-DI: 00634782002305 FDA UDI
FDA Product Code: CAE FDA UDI
GMDN Term: Oropharyngeal airway, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5110 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 80 Millimeter FDA UDI

Category: Oropharyngeal airway, reusable

Adc® by American Diagnostic Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: American Diagnostic Corporation

Sources (1)

FDA UDI 359eb317-c28a-4778-888c-af5209b48c24 36 fields · synced May 29, 2026